Team:UNIPV-Pavia/Calendar/August/week5

August, 29th

T9002-ENTERo and ENTERO-RBS were diluted 1:500 in M9 + Amp + Cm12.5 13 ml and 1 ml volume respectively. After six hour growth they were aliquoted in 96-well microplate (190 μl cultures) with 10 μl of supernatants collected on August, 27th and 10 μl of 3OC₆-HSL.
5 flasks were prepared with 29.6 ml H₂O, 200 μl glycerol 80 %, 8 ml M9 salts 5 x and their pH was adjusted to 5.9, 6.3, 6.7, 6.9 and 7.2; they were autoclaved in order to prepare M9 glycerol supplemented minimal medium.
E43-3 DNA was digested with EcorI and PstI restriction nucleases in order to screen the part length by gel-electrophoresis; it showed the correct band.

Small size gel

Plates incubated on August, 27th were all grown, except for J101-31-1C3; for each of them a colony was picked and inoculated in LB + Cm34, 5 ml, while for J101-E7 two colonies were inoculated in LB + Cm34, 5 ml.
E43-2 was again inoculated in order to screen the insert length with gel electrophoresis.

August, 30th

Glycerol stocks were prepared for E2-1C3, E3-1C3, E4-1C3, E5-1C3, E6-1C3, E7-1C3, E9-1C3, E10-1C3, E11-1C3, J101-E5-1C3, J101-E7-1C3-1 and J101-e7-1C3-2.
DNA of each culture was purified:

Each sample was digested with EcoRI and PstI endonucleases (a mix 13 x was prepared for high copy number plasmid parts):

while for E43-2 10 μl were digested. In the afternoon the parts were screened by gel electrophoresis:

Small size gel

All parts showed the correct insert length except for E3-1C3.
40 μl CaCl₂ 1M, 800 μl Casamino Acids 10 %, 80 μl MgSO₄ 1M and 1.36 ml thiamine were added to previously autoclaved flasks.